| Ophthalmic findings in Setleis syndrome: two new cases in a mother and son. | |
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MedLine Citation:
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PMID: 17508049 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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CASE REPORT: Setleis syndrome is a rare ectodermal dysplasia with characteristic ophthalmic findings. We describe the first 2 reported cases in Canadian individuals of Aboriginal descent. COMMENTS: Although most ophthalmic findings are benign, it is important to recognize the clinical significance for management and genetic counselling. We postulate an autosomal dominant inheritance in our cases. |
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Authors:
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Jerrod S Kent; Kenneth G Romanchuk; Edmond G Lemire |
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Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: Canadian journal of ophthalmology. Journal canadien d'ophtalmologie Volume: 42 ISSN: 0008-4182 ISO Abbreviation: Can. J. Ophthalmol. Publication Date: 2007 Jun |
Date Detail:
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Created Date: 2007-05-17 Completed Date: 2007-08-09 Revised Date: 2013-05-20 |
Medline Journal Info:
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Nlm Unique ID: 0045312 Medline TA: Can J Ophthalmol Country: Canada |
Other Details:
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Languages: eng Pagination: 471-3 Citation Subset: IM |
Affiliation:
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College of Medicine, University of Saskatchewan, Saskatoon, Sask. |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Adult Coloboma / diagnosis*, genetics Craniofacial Abnormalities / diagnosis*, genetics Ectodermal Dysplasia / diagnosis*, genetics Eyelashes / abnormalities* Eyelids / abnormalities* Female Genes, Dominant Humans Infant Male Skin Abnormalities / diagnosis*, genetics Syndrome |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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